Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,659 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,659 in last 12 months

Showing 2530125320 of 55,896 recalls

Medical DeviceApril 18, 2019· Stryker Neurovascular

Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to A design...

The Issue: A design related issue can contribute to the device exhibiting brittle...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...

The Issue: Incorrect raw material used by the supplier in the manufacturing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...

The Issue: Incorrect raw material used by the supplier in the manufacturing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...

The Issue: Incorrect raw material used by the supplier in the manufacturing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...

The Issue: Incorrect raw material used by the supplier in the manufacturing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Skytron, Div. The KMW Group, Inc

Recalled Item: Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam...

The Issue: Weld attaching the air heater assembly to the main sterilizer unit has shown...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-T 48002 Bridge Kit Material: 709000444 Recalled by Maquet...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 7005 UAMC Pediatric ECC Pack Material: 701051515...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Zimmer Biomet, Inc.

Recalled Item: Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by...

The Issue: Incorrect raw material used by the supplier in the manufacturing of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing